Panax Ginseng Protects Against Doxorubicin-Induced Testicular Injury in Male Rats by Modulating NF-κB/COX-2 and AR Pathways

ArticleAçık Erişim

Özet

Panax ginseng (PG) is a medicinal plant used for many years to treat many diseases. The current study aimed to investigate the possible prophylactic and therapeutic effects of PG extract on doxorubicin (DOX)-induced testicular toxicity in rats. 32 adult male Sprague–Dawley rats (200–250 g) were used in the experiment. The experimental groups were designed as control (normal saline, intraperitoneal), DOX (18 mg/kg, intraperitoneal), PG (200 mg/kg, gavage), and PG + DOX (200 mg/kg, gavage). After treatment, serum levels of testosterone, interleukin-1β (IL-1β), glutathione (GSH), luteinizing hormone (LH), superoxide dismutase (SOD), lactate dehydrogenase (LDH), catalase (CAT), follicle stimulating hormone (FSH), tumor necrosis factor-α (TNF-α), and malondialdehyde (MDA) were measured. Then, gene expression, histopathological, and immunohistochemical analyses were performed on testicular tissues. Compared to DOX, treatment with PG + DOX showed a significant improvement in serum levels of FSH, testosterone, LH, TNF-α, IL-1β, MDA, SOD, LDH, GSH, and CAT. It was also observed that PG + DOX decreased nuclear factor-κB and cyclooxygenase-2 expression levels, increased androgen receptor expression, restored testicular histopathological structure, and significantly improved spermatogenesis. The results of the present study showed that PG may have an ameliorative effect against DOX-induced male reproductive toxicity, as DOX causes male reproductive toxicity. It can be concluded that PG is one of the effects that protect against DOX-induced testicular toxicity in rats by reducing lipid peroxidation and activating the antioxidant system. In light of this information, PG may be a useful agent to prevent the testicular toxicity observed in men receiving DOX treatment. © The Author(s) 2025.

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RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/10921Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.1007/s12035-025-05116-9Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorYeni, Yesim
dc.contributor.authorCicek, Betul
dc.contributor.authorHacimuftuoglu, Ahmet
dc.contributor.authorOzkaraca, Mustafa
dc.contributor.authorMokhtare, Behzad
dc.date.accessioned2026-10-18T20:26:02.029084615Z
dc.date.available2026-10-18T20:26:02.029084615Z
dc.date.issued2025
dc.description.abstractPanax ginseng (PG) is a medicinal plant used for many years to treat many diseases. The current study aimed to investigate the possible prophylactic and therapeutic effects of PG extract on doxorubicin (DOX)-induced testicular toxicity in rats. 32 adult male Sprague–Dawley rats (200–250 g) were used in the experiment. The experimental groups were designed as control (normal saline, intraperitoneal), DOX (18 mg/kg, intraperitoneal), PG (200 mg/kg, gavage), and PG + DOX (200 mg/kg, gavage). After treatment, serum levels of testosterone, interleukin-1β (IL-1β), glutathione (GSH), luteinizing hormone (LH), superoxide dismutase (SOD), lactate dehydrogenase (LDH), catalase (CAT), follicle stimulating hormone (FSH), tumor necrosis factor-α (TNF-α), and malondialdehyde (MDA) were measured. Then, gene expression, histopathological, and immunohistochemical analyses were performed on testicular tissues. Compared to DOX, treatment with PG + DOX showed a significant improvement in serum levels of FSH, testosterone, LH, TNF-α, IL-1β, MDA, SOD, LDH, GSH, and CAT. It was also observed that PG + DOX decreased nuclear factor-κB and cyclooxygenase-2 expression levels, increased androgen receptor expression, restored testicular histopathological structure, and significantly improved spermatogenesis. The results of the present study showed that PG may have an ameliorative effect against DOX-induced male reproductive toxicity, as DOX causes male reproductive toxicity. It can be concluded that PG is one of the effects that protect against DOX-induced testicular toxicity in rats by reducing lipid peroxidation and activating the antioxidant system. In light of this information, PG may be a useful agent to prevent the testicular toxicity observed in men receiving DOX treatment. © The Author(s) 2025.
dc.description.sponsorshipOpen access funding provided by the Scientific and Technological Research Council of T\u00FCrkiye (T\u00DCB\u0130TAK). The authors did not receive any financial support.
dc.identifier.doi10.1007/s12035-025-05116-9
dc.identifier.eissn1559-1182
dc.identifier.endpage12850
dc.identifier.issn0893-7648
dc.identifier.issue10
dc.identifier.pmcidPMC12433337
dc.identifier.pmid40451973
dc.identifier.scopus2-s2.0-105006903736
dc.identifier.startpage12839
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/10921
dc.identifier.volume62
dc.identifier.wosWOS:001499384700001
dc.language.isoen
dc.publisherSpringer
dc.relation.ispartofMolecular Neurobiology
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectDoxorubicin
dc.subjectMale Fertility
dc.subjectOxidative Stress
dc.subjectPanax Ginseng
dc.subjectReal-Time PCR
dc.subjectAnimals
dc.subjectCyclooxygenase 2
dc.subjectMale
dc.subjectMalondialdehyde
dc.subjectNF-kappa B
dc.subjectPanax
dc.subjectPlant Extracts
dc.subjectProtective Agents
dc.subjectRats
dc.subjectRats, Sprague-Dawley
dc.subjectReceptors, Androgen
dc.subjectSignal Transduction
dc.subjectTestis
dc.subjectTestosterone
dc.subjectantioxidant
dc.subjectcatalase
dc.subjectfollitropin
dc.subjectginseng extract
dc.subjectglutathione
dc.subjectinterleukin 1beta
dc.subjectlactate dehydrogenase
dc.subjectluteinizing hormone
dc.subjectmalonaldehyde
dc.subjectsuperoxide dismutase
dc.subjectthiopental
dc.titlePanax Ginseng Protects Against Doxorubicin-Induced Testicular Injury in Male Rats by Modulating NF-κB/COX-2 and AR Pathways
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus3
rdl.citation.wos4
rdl.departmentFaculty of Medicine, Department of Physiology, Erzincan Binali Yildirim University, Erzincan, Turkey.
rdl.oa.statusgold
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)